Mega Lifesciences PCL
영양 보충제와 의료 자산을 유통하는 지역 웰니스 공급업체
Mega Lifesciences PCL은 비타민과 의약품에 대해 고도로 통제된 유통 체인을 운영합니다. 이 회사는 개발도상국에 안전한 의료 제품을 제공하기 위해 제조 시설과 협력하고 있습니다. 이들의 물류 자산은 엄격한 글로벌 제약 표준을 충족합니다.
- Type
- distributor (our classification of the record, not a statement by the company)
- Role
- Distributor
- Location
- Bangkok, Thailand
- Founded
- 1982
- Website
- megawecare.com
- Categories
- 보충제 및 웰니스, 의료 및 건강 관리 용품
- Markets
- 태국, 베트남, 필리핀
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Verified facts
- corporate-mail-on-domain (green), checked 2026-08-09 Mail server of the company domain
- domain-registered (green), checked 2026-08-09 Domain registry record
- registry-activity (green), checked 2026-08-15 Thailand Department of Business Development, DBD DataWarehouse (central juristic person registry)
- financials-published (green), effective since 2025-12-31 Thailand Department of Business Development, DBD DataWarehouse (central juristic person registry)
- registry-id-verified (green), checked 2026-08-20 Thailand Department of Business Development, DBD DataWarehouse (central juristic person registry)
- debarment-clear (green), checked 2026-08-09 OpenSanctions
- sanctions-clear (green), checked 2026-08-09 OpenSanctions
Claimed certifications, not confirmed by us
- Good Manufacturing Practice
- ISO 9001, Quality Management IAF CertSearch
Import rules for these goods
- Food supplements sold in the EU follow Directive 2002/46/EC: most member states require a notification to the national authority before the first sale. European Commission (supplements)
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)